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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891222Generated: October 26, 2026

Methanol → Triethylammonium 5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-methoxyethyl)-5-methyluridine-3'-O-succinate

https://huagongshe.com/reaction/891222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSuccinic anhydrideHCID 7922—
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
Reactant2'-O-(2-Methoxyethyl)-5-methyl-uridineHCID 11243988—
SolventAcetonitrileHCID 6342—
Solvent2,6-LutidineHCID 7937—
SolventTriethylamineHCID 8471—
ProductTriethylammonium 5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-methoxyethyl)-5-methyluridine-3'-O-succinateHCID 8659394590%

Reaction Steps

2′-O-(2-methoxyethyl)-5-methyluridine (MOE T, 15.8 g, 50 mmol) was dissolved in 2,6-lutidine (23.3 ml) and acetonitrile (150 ml). 4,4′-Dimethoxytrityl chloride (DMTCl, 18.6 g, 55 mmol) was added. The mixture was stirred at room temperature for 30 min. and methanol (MeOH, 0.2 ml) was added. After 10 min., triethylamine (20 ml) and succinic anhydride (15 g) were added and the mixture was stirred overnight. The mixture was concentrated under reduced pressure. The residue was dissolved in dichloromethane (200 ml) and washed with triethylammonium phosphate (0.5 M, pH 7, 3×100 ml). The organic layer was dried (Na2SO4) and evaporated to approximately 100 ml. Hexane (150 ml) was added. The mixture was shaken for 5 min. and the supernatant was decanted. The residue was dried to give a yellow solid (36.8 g, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07002006B2
Source datasetuspto-grants-2006_02
ORD IDord-31150971ef5548aca6bcf0ff9556428b
Source noteuspto-grants-2006_02